Canonical Allele Identifier: CA1957607203
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625440G= , CM000673.2:g.22625440G= GRCh38
NC_000011.9:g.22646986G= , CM000673.1:g.22646986G= GRCh37
NC_000011.8:g.22603562G= NCBI36
NG_007425.1:g.5402C= , LRG_527:g.5402C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.371C= MANE Select ENSP00000330875.3:p.Ala124=
ENST00000327470.4:c.371C= ENSP00000330875.3:p.Ala124=
NM_022725.3:c.371C= , LRG_527t1:c.371C= NP_073562.1:p.Ala124=
NM_022725.4:c.371C= MANE Select NP_073562.1:p.Ala124=
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Search 100 bp 3'